RRMS newly diagnosed

I was diagnosed in April last year and I have had my first treatment of mavenclad but for the past three months I’ve been in a flare up and still struggling. I feel like a burden to everyone who’s looking after me I do work part time as a TA for special needs children and I love the job. I’m just so scared of loosing my partner because of my MS and not always able to do something and having to rest for days because I’m so exhausted. I just feel like a massive burden and so much guilt anyone feel this way and know of ways of trying not to feel this way?